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Clinical Country Site Lead

Biogen
Full-time
Remote friendly (United States)
United States
$131,000 - $175,000 USD yearly
Clinical Research and Development

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Role Summary

Clinical Country Site Lead (CCSL) is a field-based, country-aligned role providing local operational and scientific expertise to drive global clinical development strategy, enable local partnerships, and support country-focused delivery and execution of the R&D pipeline.

Responsibilities

  • Maintain current awareness of local clinical knowledge, emerging standards of care, and trial needs of clinicians; act as local QSDO expert to drive and support global operational strategy; coordinate cross-functional local input for Clinical Development Plan.
  • Develop and manage investigator and site knowledge/relationships to highlight country-level capabilities, needs, and satisfaction; implement a country-level QSDO investigator engagement strategy.
  • Serve as primary country-level QSDO/Biogen contact for sponsor oversight of clinical trial monitoring activities; may interact with FSP resources and support monitoring operations.
  • Act as Lead CCSL as required, including membership in CDT/ SMTs, coordinating program and study country foundations, site selection activities, and training CCSLs on therapeutic areas and program communications.
  • Lead interactions to ensure timely local information flow and resolution of issues with investigators, affiliate staff, CRO/FSP staff, and global teams; monitor Country Performance KPIs and support country milestones.
  • Lead local activities in country/site selection processes to gather input from treating physicians and stakeholders.
  • Provide operational direction for assigned associate CCSLs as needed; support special projects or other QSDO activities as a CSO/Country representative.

Qualifications

  • Required: B.A. or B.S. degree in a scientific discipline; minimum 8 years in clinical research; experience managing clinical trial activities, preferably sponsor oversight in outsourced/FSP models; strong knowledge of cross-functional drug development and ICH/GCP with regulatory familiarity; excellent project management and organizational skills; proficiency with IT tools for virtual teamwork; strong knowledge of clinical operations across local geography; customer-focused with leadership, interpersonal, and cross-cultural abilities; ability to manage multiple tasks and priorities; strong English communication skills.
  • Preferred: Advanced degree; experience in fully outsourced/FSP models.

Skills

  • Strong site management and relationship-building skills
  • Strategic thinking with ability to influence global operational plans
  • Excellent communication and collaboration across cross-functional teams
  • Ability to work remotely and build relationships across the organization

Education

  • B.A. or B.S. in a scientific discipline (required); advanced degree preferred.

Additional Requirements

  • Location and travel: Field-based role with country-focused responsibilities (travel as required for site oversight and collaboration).
  • Other: None specified.
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